Name: rs267608321
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs267608321

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:42132028-42132049 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / d…
del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₃=0.00000 (0/13186, ALFA)
del(T)₁₂=0.00000 (0/13186, ALFA)
del(T)₁₁=0.00000 (0/13186, ALFA) (+ 14 more)
del(T)₁₀=0.00000 (0/13186, ALFA)
del(T)₉=0.00000 (0/13186, ALFA)
del(T)₈=0.00000 (0/13186, ALFA)
del(T)₇=0.00000 (0/13186, ALFA)
del(T)₆=0.00000 (0/13186, ALFA)
del(T)₅=0.00000 (0/13186, ALFA)
del(T)₄=0.00000 (0/13186, ALFA)
delTTT=0.00000 (0/13186, ALFA)
delTT=0.00000 (0/13186, ALFA)
delT=0.00000 (0/13186, ALFA)
dupT=0.00000 (0/13186, ALFA)
dupTT=0.00000 (0/13186, ALFA)
dupTTT=0.00000 (0/13186, ALFA)
dup(T)₅=0.00000 (0/13186, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CYP2D6 : 2KB Upstream Variant
LOC102723722 : Intron Variant
Publications: 1 citation
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	13186	TTTTTTTTTTTTTTTTTTTTTT=1.00000	TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	9436	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2372	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	76	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	2296	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	94	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	74	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	20	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	132	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	588	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	98	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	466	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	13186	(T)₂₂=1.00000	del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00000, dupTT=0.00000, dupTTT=0.00000, dup(T)₅=0.00000
Allele Frequency Aggregator	European	Sub	9436	(T)₂₂=1.0000	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	African	Sub	2372	(T)₂₂=1.0000	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	588	(T)₂₂=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Other	Sub	466	(T)₂₂=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	132	(T)₂₂=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	South Asian	Sub	98	(T)₂₂=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	Asian	Sub	94	(T)₂₂=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₅=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 22	NC_000022.11:g.42132037_42132049del
GRCh38.p14 chr 22	NC_000022.11:g.42132038_42132049del
GRCh38.p14 chr 22	NC_000022.11:g.42132039_42132049del
GRCh38.p14 chr 22	NC_000022.11:g.42132040_42132049del
GRCh38.p14 chr 22	NC_000022.11:g.42132041_42132049del
GRCh38.p14 chr 22	NC_000022.11:g.42132042_42132049del
GRCh38.p14 chr 22	NC_000022.11:g.42132043_42132049del
GRCh38.p14 chr 22	NC_000022.11:g.42132044_42132049del
GRCh38.p14 chr 22	NC_000022.11:g.42132045_42132049del
GRCh38.p14 chr 22	NC_000022.11:g.42132046_42132049del
GRCh38.p14 chr 22	NC_000022.11:g.42132047_42132049del
GRCh38.p14 chr 22	NC_000022.11:g.42132048_42132049del
GRCh38.p14 chr 22	NC_000022.11:g.42132049del
GRCh38.p14 chr 22	NC_000022.11:g.42132049dup
GRCh38.p14 chr 22	NC_000022.11:g.42132048_42132049dup
GRCh38.p14 chr 22	NC_000022.11:g.42132047_42132049dup
GRCh38.p14 chr 22	NC_000022.11:g.42132046_42132049dup
GRCh38.p14 chr 22	NC_000022.11:g.42132045_42132049dup
GRCh38.p14 chr 22	NC_000022.11:g.42132044_42132049dup
GRCh38.p14 chr 22	NC_000022.11:g.42132043_42132049dup
GRCh38.p14 chr 22	NC_000022.11:g.42132042_42132049dup
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3771_3783del
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3772_3783del
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3773_3783del
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3774_3783del
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3775_3783del
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3776_3783del
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3777_3783del
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3778_3783del
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3779_3783del
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3780_3783del
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3781_3783del
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3782_3783del
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3783del
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3783dup
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3782_3783dup
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3781_3783dup
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3780_3783dup
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3779_3783dup
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3778_3783dup
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3777_3783dup
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3776_3783dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9780_9792del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9781_9792del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9782_9792del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9783_9792del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9784_9792del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9785_9792del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9786_9792del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9787_9792del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9788_9792del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9789_9792del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9790_9792del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9791_9792del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9792del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9792dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9791_9792dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9790_9792dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9789_9792dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9788_9792dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9787_9792dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9786_9792dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9785_9792dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25628_25640del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25629_25640del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25630_25640del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25631_25640del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25632_25640del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25633_25640del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25634_25640del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25635_25640del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25636_25640del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25637_25640del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25638_25640del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25639_25640del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25640del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25640dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25639_25640dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25638_25640dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25637_25640dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25636_25640dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25635_25640dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25634_25640dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25633_25640dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17605_17617del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17606_17617del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17607_17617del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17608_17617del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17609_17617del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17610_17617del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17611_17617del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17612_17617del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17613_17617del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17614_17617del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17615_17617del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17616_17617del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17617del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17617dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17616_17617dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17615_17617dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17614_17617dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17613_17617dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17612_17617dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17611_17617dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17610_17617dup
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54367_54379del
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54368_54379del
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54369_54379del
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54370_54379del
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54371_54379del
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54372_54379del
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54373_54379del
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54374_54379del
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54375_54379del
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54376_54379del
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54377_54379del
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54378_54379del
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54379del
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54379dup
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54378_54379dup
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54377_54379dup
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54376_54379dup
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54375_54379dup
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54374_54379dup
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54373_54379dup
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54372_54379dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54383_54395del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54384_54395del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54385_54395del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54386_54395del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54387_54395del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54388_54395del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54389_54395del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54390_54395del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54391_54395del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54392_54395del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54393_54395del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54394_54395del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54395del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54395dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54394_54395dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54393_54395dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54392_54395dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54391_54395dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54390_54395dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54389_54395dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54388_54395dup
GRCh37.p13 chr 22	NC_000022.10:g.42528044_42528056del
GRCh37.p13 chr 22	NC_000022.10:g.42528045_42528056del
GRCh37.p13 chr 22	NC_000022.10:g.42528046_42528056del
GRCh37.p13 chr 22	NC_000022.10:g.42528047_42528056del
GRCh37.p13 chr 22	NC_000022.10:g.42528048_42528056del
GRCh37.p13 chr 22	NC_000022.10:g.42528049_42528056del
GRCh37.p13 chr 22	NC_000022.10:g.42528050_42528056del
GRCh37.p13 chr 22	NC_000022.10:g.42528051_42528056del
GRCh37.p13 chr 22	NC_000022.10:g.42528052_42528056del
GRCh37.p13 chr 22	NC_000022.10:g.42528053_42528056del
GRCh37.p13 chr 22	NC_000022.10:g.42528054_42528056del
GRCh37.p13 chr 22	NC_000022.10:g.42528055_42528056del
GRCh37.p13 chr 22	NC_000022.10:g.42528056del
GRCh37.p13 chr 22	NC_000022.10:g.42528056dup
GRCh37.p13 chr 22	NC_000022.10:g.42528055_42528056dup
GRCh37.p13 chr 22	NC_000022.10:g.42528054_42528056dup
GRCh37.p13 chr 22	NC_000022.10:g.42528053_42528056dup
GRCh37.p13 chr 22	NC_000022.10:g.42528052_42528056dup
GRCh37.p13 chr 22	NC_000022.10:g.42528051_42528056dup
GRCh37.p13 chr 22	NC_000022.10:g.42528050_42528056dup
GRCh37.p13 chr 22	NC_000022.10:g.42528049_42528056dup
LOC110740340 genomic region	NG_055460.1:g.1322_1334del
LOC110740340 genomic region	NG_055460.1:g.1323_1334del
LOC110740340 genomic region	NG_055460.1:g.1324_1334del
LOC110740340 genomic region	NG_055460.1:g.1325_1334del
LOC110740340 genomic region	NG_055460.1:g.1326_1334del
LOC110740340 genomic region	NG_055460.1:g.1327_1334del
LOC110740340 genomic region	NG_055460.1:g.1328_1334del
LOC110740340 genomic region	NG_055460.1:g.1329_1334del
LOC110740340 genomic region	NG_055460.1:g.1330_1334del
LOC110740340 genomic region	NG_055460.1:g.1331_1334del
LOC110740340 genomic region	NG_055460.1:g.1332_1334del
LOC110740340 genomic region	NG_055460.1:g.1333_1334del
LOC110740340 genomic region	NG_055460.1:g.1334del
LOC110740340 genomic region	NG_055460.1:g.1334dup
LOC110740340 genomic region	NG_055460.1:g.1333_1334dup
LOC110740340 genomic region	NG_055460.1:g.1332_1334dup
LOC110740340 genomic region	NG_055460.1:g.1331_1334dup
LOC110740340 genomic region	NG_055460.1:g.1330_1334dup
LOC110740340 genomic region	NG_055460.1:g.1329_1334dup
LOC110740340 genomic region	NG_055460.1:g.1328_1334dup
LOC110740340 genomic region	NG_055460.1:g.1327_1334dup

Gene: CYP2D6, cytochrome P450 family 2 subfamily D member 6 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
CYP2D6 transcript variant 1	NM_000106.6:c.	N/A	Upstream Transcript Variant
CYP2D6 transcript variant 2	NM_001025161.3:c.	N/A	Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₂=	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈
GRCh38.p14 chr 22	NC_000022.11:g.42132028_42132049=	NC_000022.11:g.42132037_42132049del	NC_000022.11:g.42132038_42132049del	NC_000022.11:g.42132039_42132049del	NC_000022.11:g.42132040_42132049del	NC_000022.11:g.42132041_42132049del	NC_000022.11:g.42132042_42132049del	NC_000022.11:g.42132043_42132049del	NC_000022.11:g.42132044_42132049del	NC_000022.11:g.42132045_42132049del	NC_000022.11:g.42132046_42132049del	NC_000022.11:g.42132047_42132049del	NC_000022.11:g.42132048_42132049del	NC_000022.11:g.42132049del	NC_000022.11:g.42132049dup	NC_000022.11:g.42132048_42132049dup	NC_000022.11:g.42132047_42132049dup	NC_000022.11:g.42132046_42132049dup	NC_000022.11:g.42132045_42132049dup	NC_000022.11:g.42132044_42132049dup	NC_000022.11:g.42132043_42132049dup	NC_000022.11:g.42132042_42132049dup
gene/pseudogene RefSeqGene (LRG_303)	NG_008376.4:g.3762_3783=	NG_008376.4:g.3771_3783del	NG_008376.4:g.3772_3783del	NG_008376.4:g.3773_3783del	NG_008376.4:g.3774_3783del	NG_008376.4:g.3775_3783del	NG_008376.4:g.3776_3783del	NG_008376.4:g.3777_3783del	NG_008376.4:g.3778_3783del	NG_008376.4:g.3779_3783del	NG_008376.4:g.3780_3783del	NG_008376.4:g.3781_3783del	NG_008376.4:g.3782_3783del	NG_008376.4:g.3783del	NG_008376.4:g.3783dup	NG_008376.4:g.3782_3783dup	NG_008376.4:g.3781_3783dup	NG_008376.4:g.3780_3783dup	NG_008376.4:g.3779_3783dup	NG_008376.4:g.3778_3783dup	NG_008376.4:g.3777_3783dup	NG_008376.4:g.3776_3783dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.9769_9792=	NW_015148968.1:g.9780_9792del	NW_015148968.1:g.9781_9792del	NW_015148968.1:g.9782_9792del	NW_015148968.1:g.9783_9792del	NW_015148968.1:g.9784_9792del	NW_015148968.1:g.9785_9792del	NW_015148968.1:g.9786_9792del	NW_015148968.1:g.9787_9792del	NW_015148968.1:g.9788_9792del	NW_015148968.1:g.9789_9792del	NW_015148968.1:g.9790_9792del	NW_015148968.1:g.9791_9792del	NW_015148968.1:g.9792del	NW_015148968.1:g.9792dup	NW_015148968.1:g.9791_9792dup	NW_015148968.1:g.9790_9792dup	NW_015148968.1:g.9789_9792dup	NW_015148968.1:g.9788_9792dup	NW_015148968.1:g.9787_9792dup	NW_015148968.1:g.9786_9792dup	NW_015148968.1:g.9785_9792dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.25617_25640=	NW_014040931.1:g.25628_25640del	NW_014040931.1:g.25629_25640del	NW_014040931.1:g.25630_25640del	NW_014040931.1:g.25631_25640del	NW_014040931.1:g.25632_25640del	NW_014040931.1:g.25633_25640del	NW_014040931.1:g.25634_25640del	NW_014040931.1:g.25635_25640del	NW_014040931.1:g.25636_25640del	NW_014040931.1:g.25637_25640del	NW_014040931.1:g.25638_25640del	NW_014040931.1:g.25639_25640del	NW_014040931.1:g.25640del	NW_014040931.1:g.25640dup	NW_014040931.1:g.25639_25640dup	NW_014040931.1:g.25638_25640dup	NW_014040931.1:g.25637_25640dup	NW_014040931.1:g.25636_25640dup	NW_014040931.1:g.25635_25640dup	NW_014040931.1:g.25634_25640dup	NW_014040931.1:g.25633_25640dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.17594_17617=	NW_009646208.1:g.17605_17617del	NW_009646208.1:g.17606_17617del	NW_009646208.1:g.17607_17617del	NW_009646208.1:g.17608_17617del	NW_009646208.1:g.17609_17617del	NW_009646208.1:g.17610_17617del	NW_009646208.1:g.17611_17617del	NW_009646208.1:g.17612_17617del	NW_009646208.1:g.17613_17617del	NW_009646208.1:g.17614_17617del	NW_009646208.1:g.17615_17617del	NW_009646208.1:g.17616_17617del	NW_009646208.1:g.17617del	NW_009646208.1:g.17617dup	NW_009646208.1:g.17616_17617dup	NW_009646208.1:g.17615_17617dup	NW_009646208.1:g.17614_17617dup	NW_009646208.1:g.17613_17617dup	NW_009646208.1:g.17612_17617dup	NW_009646208.1:g.17611_17617dup	NW_009646208.1:g.17610_17617dup
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1	NW_004504305.1:g.54355_54379=	NW_004504305.1:g.54367_54379del	NW_004504305.1:g.54368_54379del	NW_004504305.1:g.54369_54379del	NW_004504305.1:g.54370_54379del	NW_004504305.1:g.54371_54379del	NW_004504305.1:g.54372_54379del	NW_004504305.1:g.54373_54379del	NW_004504305.1:g.54374_54379del	NW_004504305.1:g.54375_54379del	NW_004504305.1:g.54376_54379del	NW_004504305.1:g.54377_54379del	NW_004504305.1:g.54378_54379del	NW_004504305.1:g.54379del	NW_004504305.1:g.54379dup	NW_004504305.1:g.54378_54379dup	NW_004504305.1:g.54377_54379dup	NW_004504305.1:g.54376_54379dup	NW_004504305.1:g.54375_54379dup	NW_004504305.1:g.54374_54379dup	NW_004504305.1:g.54373_54379dup	NW_004504305.1:g.54372_54379dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.54369_54395=	NT_187682.1:g.54383_54395del	NT_187682.1:g.54384_54395del	NT_187682.1:g.54385_54395del	NT_187682.1:g.54386_54395del	NT_187682.1:g.54387_54395del	NT_187682.1:g.54388_54395del	NT_187682.1:g.54389_54395del	NT_187682.1:g.54390_54395del	NT_187682.1:g.54391_54395del	NT_187682.1:g.54392_54395del	NT_187682.1:g.54393_54395del	NT_187682.1:g.54394_54395del	NT_187682.1:g.54395del	NT_187682.1:g.54395dup	NT_187682.1:g.54394_54395dup	NT_187682.1:g.54393_54395dup	NT_187682.1:g.54392_54395dup	NT_187682.1:g.54391_54395dup	NT_187682.1:g.54390_54395dup	NT_187682.1:g.54389_54395dup	NT_187682.1:g.54388_54395dup
GRCh37.p13 chr 22	NC_000022.10:g.42528030_42528056=	NC_000022.10:g.42528044_42528056del	NC_000022.10:g.42528045_42528056del	NC_000022.10:g.42528046_42528056del	NC_000022.10:g.42528047_42528056del	NC_000022.10:g.42528048_42528056del	NC_000022.10:g.42528049_42528056del	NC_000022.10:g.42528050_42528056del	NC_000022.10:g.42528051_42528056del	NC_000022.10:g.42528052_42528056del	NC_000022.10:g.42528053_42528056del	NC_000022.10:g.42528054_42528056del	NC_000022.10:g.42528055_42528056del	NC_000022.10:g.42528056del	NC_000022.10:g.42528056dup	NC_000022.10:g.42528055_42528056dup	NC_000022.10:g.42528054_42528056dup	NC_000022.10:g.42528053_42528056dup	NC_000022.10:g.42528052_42528056dup	NC_000022.10:g.42528051_42528056dup	NC_000022.10:g.42528050_42528056dup	NC_000022.10:g.42528049_42528056dup
LOC110740340 genomic region	NG_055460.1:g.1313_1334=	NG_055460.1:g.1322_1334del	NG_055460.1:g.1323_1334del	NG_055460.1:g.1324_1334del	NG_055460.1:g.1325_1334del	NG_055460.1:g.1326_1334del	NG_055460.1:g.1327_1334del	NG_055460.1:g.1328_1334del	NG_055460.1:g.1329_1334del	NG_055460.1:g.1330_1334del	NG_055460.1:g.1331_1334del	NG_055460.1:g.1332_1334del	NG_055460.1:g.1333_1334del	NG_055460.1:g.1334del	NG_055460.1:g.1334dup	NG_055460.1:g.1333_1334dup	NG_055460.1:g.1332_1334dup	NG_055460.1:g.1331_1334dup	NG_055460.1:g.1330_1334dup	NG_055460.1:g.1329_1334dup	NG_055460.1:g.1328_1334dup	NG_055460.1:g.1327_1334dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

35 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	CMH_GENOMICS	ss538296142	Mar 11, 2015 (142)
2	KOGIC	ss3983733712	Apr 27, 2020 (154)
3	KOGIC	ss3983733713	Apr 27, 2020 (154)
4	GNOMAD	ss4365370590	Apr 26, 2021 (155)
5	GNOMAD	ss4365370591	Apr 26, 2021 (155)
6	GNOMAD	ss4365370592	Apr 26, 2021 (155)
7	GNOMAD	ss4365370593	Apr 26, 2021 (155)
8	GNOMAD	ss4365370594	Apr 26, 2021 (155)
9	GNOMAD	ss4365370595	Apr 26, 2021 (155)
10	GNOMAD	ss4365370596	Apr 26, 2021 (155)
11	GNOMAD	ss4365370597	Apr 26, 2021 (155)
12	GNOMAD	ss4365370598	Apr 26, 2021 (155)
13	GNOMAD	ss4365370599	Apr 26, 2021 (155)
14	GNOMAD	ss4365370600	Apr 26, 2021 (155)
15	GNOMAD	ss4365370601	Apr 26, 2021 (155)
16	GNOMAD	ss4365370602	Apr 26, 2021 (155)
17	GNOMAD	ss4365370603	Apr 26, 2021 (155)
18	GNOMAD	ss4365370604	Apr 26, 2021 (155)
19	GNOMAD	ss4365370605	Apr 26, 2021 (155)
20	GNOMAD	ss4365370606	Apr 26, 2021 (155)
21	GNOMAD	ss4365370607	Apr 26, 2021 (155)
22	GNOMAD	ss4365370608	Apr 26, 2021 (155)
23	TOPMED	ss5110781909	Apr 26, 2021 (155)
24	TOPMED	ss5110781910	Apr 26, 2021 (155)
25	TOPMED	ss5110781911	Apr 26, 2021 (155)
26	TOPMED	ss5110781912	Apr 26, 2021 (155)
27	1000G_HIGH_COVERAGE	ss5311255815	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5311255816	Oct 16, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5311255817	Oct 16, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5311255818	Oct 16, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5311255819	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5503082787	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5503082789	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5794029429	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5794029431	Oct 16, 2022 (156)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571271047 (NC_000022.11:42132027::T 3187/112054) Row 571271048 (NC_000022.11:42132027::TT 146/112600) Row 571271049 (NC_000022.11:42132027::TTT 13/112674)...	-	Apr 26, 2021 (155)
56	Korean Genome Project Submission ignored due to conflicting rows: Row 40111713 (NC_000022.11:42132031::T 30/1006) Row 40111714 (NC_000022.11:42132030:T: 87/1006)	-	Apr 27, 2020 (154)
57	Korean Genome Project Submission ignored due to conflicting rows: Row 40111713 (NC_000022.11:42132031::T 30/1006) Row 40111714 (NC_000022.11:42132030:T: 87/1006)	-	Apr 27, 2020 (154)
58	14KJPN Submission ignored due to conflicting rows: Row 127866533 (NC_000022.11:42132027::T 516/25484) Row 127866535 (NC_000022.11:42132027:T: 38/25484)	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 127866533 (NC_000022.11:42132027::T 516/25484) Row 127866535 (NC_000022.11:42132027:T: 38/25484)	-	Oct 16, 2022 (156)
60	TopMed Submission ignored due to conflicting rows: Row 385890856 (NC_000022.11:42132027:TTTTTTTTTT: 3/264690) Row 385890857 (NC_000022.11:42132027:TTTTTTTTTTT: 7/264690) Row 385890858 (NC_000022.11:42132027:TTTTTTTTTTTT: 7/264690)...	-	Apr 26, 2021 (155)
61	TopMed Submission ignored due to conflicting rows: Row 385890856 (NC_000022.11:42132027:TTTTTTTTTT: 3/264690) Row 385890857 (NC_000022.11:42132027:TTTTTTTTTTT: 7/264690) Row 385890858 (NC_000022.11:42132027:TTTTTTTTTTTT: 7/264690)...	-	Apr 26, 2021 (155)
62	TopMed Submission ignored due to conflicting rows: Row 385890856 (NC_000022.11:42132027:TTTTTTTTTT: 3/264690) Row 385890857 (NC_000022.11:42132027:TTTTTTTTTTT: 7/264690) Row 385890858 (NC_000022.11:42132027:TTTTTTTTTTTT: 7/264690)...	-	Apr 26, 2021 (155)
63	TopMed Submission ignored due to conflicting rows: Row 385890856 (NC_000022.11:42132027:TTTTTTTTTT: 3/264690) Row 385890857 (NC_000022.11:42132027:TTTTTTTTTTT: 7/264690) Row 385890858 (NC_000022.11:42132027:TTTTTTTTTTTT: 7/264690)...	-	Apr 26, 2021 (155)
64	ALFA	NC_000022.11 - 42132028	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5110781912	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTT:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4365370608, ss5110781911	NC_000022.11:42132027:TTTTTTTTTTTT:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4365370607, ss5110781910	NC_000022.11:42132027:TTTTTTTTTTT:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4365370606, ss5110781909	NC_000022.11:42132027:TTTTTTTTTT:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4365370605	NC_000022.11:42132027:TTTTTTTTT:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4365370604	NC_000022.11:42132027:TTTTTTTT:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4365370603, ss5311255818	NC_000022.11:42132027:TTTTTTT:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4365370602	NC_000022.11:42132027:TTTTTT:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4365370601	NC_000022.11:42132027:TTTTT:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4365370600, ss5311255819	NC_000022.11:42132027:TTTT:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4365370599	NC_000022.11:42132027:TTT:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss538296142, ss4365370598	NC_000022.11:42132027:TT:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5311255816, ss5503082789, ss5794029431	NC_000022.11:42132027:T:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3983733713	NC_000022.11:42132030:T:	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4365370590, ss5311255815, ss5503082787, ss5794029429	NC_000022.11:42132027::T	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3983733712	NC_000022.11:42132031::T	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365370591, ss5311255817	NC_000022.11:42132027::TT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365370592	NC_000022.11:42132027::TTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365370593	NC_000022.11:42132027::TTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365370594	NC_000022.11:42132027::TTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3716048346	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365370595	NC_000022.11:42132027::TTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365370596	NC_000022.11:42132027::TTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365370597	NC_000022.11:42132027::TTTTTTTT	NC_000022.11:42132027:TTTTTTTTTTTT… NC_000022.11:42132027:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

1 citation for rs267608321

PMID	Title	Author	Year	Journal
15768052	Identification and characterization of novel sequence variations in the cytochrome P4502D6 (CYP2D6) gene in African Americans.	Gaedigk A et al.	2005	The pharmacogenomics journal

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs267608321